![Boron, difluoro[3-[(2-quinolyl-κN)amino]-1H-isoindol-1-onato-κN2]-, (T-4)-](https://resource.bocsci.com/structure/1519003-31-6.gif)
Boron, difluoro[3-[(2-quinolyl-κN)amino]-1H-isoindol-1-onato-κN2]-, (T-4)- | CAS 1519003-31-6
| Catalog Number | F01-0116 |
| Category | BODIPY |
| Molecular Formula | C17H10BF2N3O |
| Molecular Weight | 321.094 |
* Please be kindly noted products are not for therapeutic use. We do not sell to patients.
Product Introduction
Premium BODIPY-based fluorescent probe for precise bioimaging and cell labeling. As a trusted fluorescent dye supplier, we offer high-purity dyes for researchers looking to buy fluorescent dyes online with excellent brightness and stability.
Product Specification
Application
| Excitation | 649 |
| Emission | 667 |
| Storage | Store at -20°C |
Boron difluoro[3-[(2-quinolyl-κN)amino]-1H-isoindol-1-onato-κN2]- (T-4) is a synthetic compound with potential applications in material science and chemical research.
Luminescent Materials: This boron-based compound can be used in the development of luminescent materials for advanced optical devices. Its distinct electronic properties enable it to emit light when excited, making it valuable for applications in organic light-emitting diodes (OLEDs) and other display technologies. Researchers explore its utility in creating more efficient and durable lighting solutions.
Sensors and Detection: The unique structural features of this compound facilitate its use in chemical sensors. It can be engineered to detect specific ions or molecules, aiding in environmental monitoring and industrial process control. By incorporating it into sensor platforms, scientists can enhance selectivity and sensitivity for various analytical applications.
Catalysis: Boron difluoro compounds are of interest in the field of catalysis due to their ability to facilitate organic transformations. This particular compound can serve as a catalyst in reactions that require the activation of small molecules, such as hydrogenation and hydroboration processes. Its catalytic activity is explored to develop more sustainable and efficient chemical manufacturing methods.
Phosphorescent Probes: The compound's strong phosphorescent properties make it suitable for designing phosphorescent probes for biological imaging. These probes can be utilized in cellular and molecular imaging to study biological processes with high sensitivity and resolution. This aids researchers in visualizing interactions and phenomena within biological systems for clinical and diagnostic purposes.
Recommended Services
Recommended Articles
- Hoechst Dyes: Definition, Structure, Mechanism and Applications
- Mastering the Spectrum: A Comprehensive Guide to Cy3 and Cy5 Dyes
- Fluorescent Probes: Definition, Structure, Types and Application
- Fluorescent Dyes: Definition, Mechanism, Types and Application
- Coumarin Dyes: Definition, Structure, Benefits, Synthesis and Uses
- Unlocking the Power of Fluorescence Imaging: A Comprehensive Guide
- Cell Imaging: Definitions, Systems, Protocols, Dyes, and Applications
- Lipid Staining: Definition, Principles, Methods, Dyes, and Uses
- Flow Cytometry: Definition, Principles, Protocols, Dyes, and Uses
- Nucleic Acid Staining: Definition, Principles, Dyes, Procedures, and Uses
Recommended Products
Online Inquiry